Allele Registry

Canonical Allele Identifier: PA2825084071

Gene: CFI HGNC NCBI

ClinVar Allele:

3395098

ClinVar RCV:

RCV004555240

ClinVar Variation:

3235979

HGVS (amino-acid)	Matching Registered Transcripts
NP_000195.3:p.Asp524Gly	CA357854665 NM_000204.5:c.1571A>G